Successful Treatment of Systemic Lupus Erythematosus Cerebritis with Intravenous Immunoglobulin
Identifieur interne : 002639 ( Main/Exploration ); précédent : 002638; suivant : 002640Successful Treatment of Systemic Lupus Erythematosus Cerebritis with Intravenous Immunoglobulin
Auteurs : Y. Sherer [États-Unis] ; Y. Levy [États-Unis] ; P. Langevitz [États-Unis] ; M. Lorber [États-Unis] ; F. Fabrizzi ; Y. Shoenfeld [États-Unis]Source :
- Clinical Rheumatology [ 0770-3198 ] ; 1999-04-01.
English descriptors
Abstract
Abstract:: Neuropsychiatric lupus includes extremely diverse clinical manifestations, ranging from mild cognitive dysfunction to a severe, life-threatening presentation. We report a 28-year-old patient with systemic lupus erythematosus who had persistent fever for 3 months, and developed within a few hours motor and sensory aphasia, rotator nystagmus with deviation of the eyes, and severe nuchal rigitidy. An extensive series of imaging and laboratory tests were interpreted as normal, except for an elevated opening pressure at lumbar puncture, cerebrospinal fluid inflammatory findings, and asymmetrical cortical perfusion on single-photon emission computed tomography. The patient received one course of high-dose intravenous immunoglobulin (IVIg) and within 5 days her condition returned to that of 3 months before admission. The mechanisms of injury, along with the management of cerebral lupus and the mechanisms of action of IVIg, are discussed.
Url:
DOI: 10.1007/s100670050079
Affiliations:
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<front><div type="abstract" xml:lang="en">Abstract:: Neuropsychiatric lupus includes extremely diverse clinical manifestations, ranging from mild cognitive dysfunction to a severe, life-threatening presentation. We report a 28-year-old patient with systemic lupus erythematosus who had persistent fever for 3 months, and developed within a few hours motor and sensory aphasia, rotator nystagmus with deviation of the eyes, and severe nuchal rigitidy. An extensive series of imaging and laboratory tests were interpreted as normal, except for an elevated opening pressure at lumbar puncture, cerebrospinal fluid inflammatory findings, and asymmetrical cortical perfusion on single-photon emission computed tomography. The patient received one course of high-dose intravenous immunoglobulin (IVIg) and within 5 days her condition returned to that of 3 months before admission. The mechanisms of injury, along with the management of cerebral lupus and the mechanisms of action of IVIg, are discussed.</div>
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